A Level Organic Chemistry Flashcards

1
Q

Name the reagents and conditions for the conversion of Halogenoalkanes (R-X) to Alcohols (R-OH)

A

Reagent: NaOH (aq)
Conditions: Heat

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2
Q

Name the reagents and conditions for the conversion of Halogenoalkanes (R-X) to Nitriles (R-CN)

A

Reagent: KCN (in ethanol)
Conditions: Heat under reflux

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3
Q

Name the reagents and conditions for the conversion of Halogenoalkanes (R-X) to Amines (R-NH2)

A

Reagent: Excess NH3 (in ethanol)
Conditions: Heat AND Pressure

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4
Q

Name the reagents and conditions for the conversion of Alkanes (R-H) to Halogenoalkanes (R-X)

A

Reagent: Br2
Conditions: UV

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5
Q

Name the reagents and conditions for the conversion of Benzene/Arenes to Cycloalkanes

A

Reagent: H2
Conditions: Ni/Pt Catalyst

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6
Q

Name the reagents and conditions for the conversion of Benzene to Halogenoarenes

A

Reagents: Cl2
Conditions: Anhydrous AlCl3 catalyst

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7
Q

Name the reagents and conditions for the halogenation of side chain of alkylbenzene

A

Reagents: Cl2
Conditions: UV light

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8
Q

Name the reagents and conditions for the nitration of benzene

A

Reagents: Conc. HNO3 + Conc. H2SO4
Conditions: Reflux at 25°C to 60°C

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9
Q

Name the reagents and conditions for the alkylation of benzene

A

Reagents: Halogenoalkanes (R-X)
Conditions: AlCl3 catalyst + Heat

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10
Q

Name the reagents and conditions for the acylation of benzene

A

Reagents: Acyl chlorides (R-COCl)
Conditions: AlCl3 catalyst + Heat

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11
Q

Name the reagents and conditions for the oxidation of the side-chain in arenes to produce benzoic acid

A

Reagents: Alkaline KMnO4 + Dilute H2SO4
Conditions: Heat under reflux

*NOTE: no matter what the alkyl group is methyl, ethyl or hexyl the product is always going to be benzoic acid

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12
Q

Name the reagents and conditions for the diazotization reaction

A

Reagents: Phenylamine + HNO2 + dilute HCl
Conditions: T<10°C

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13
Q

Name the reagents and conditions for the production of phenol from diazonium salt

A

Reagents: H2O
Conditions: Warm

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14
Q

Name the reagents and conditions for the bromination of phenol

A

Reagents: Br2
Conditions: Room Temperature

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15
Q

Name the reagents and conditions for the nitration of phenol to give 2-nitrophenol and 4-nitrophenol

A

Reagents: Dilute HNO3
Conditions: Room Temperature

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16
Q

Name the reagents and conditions for the nitration of phenol to give 2,4,6-trinitrophenol

A

Reagents: Conc. HNO3
Conditions: Room Temperature

17
Q

Name the reagents and conditions for the coupling reaction between diazonium salts and phenol

A

Reagents: Phenol (in NaOH) + Diazonium Salts
Conditions: T<10°C

18
Q

Name the reagents and conditions for the preparation of acyl chlorides from carboxylic acids using PCl5

A

Reagents: PCl5
Conditions: No Special Conditions

19
Q

Name the reagents and conditions for the preparation of acyl chlorides from carboxylic acids using PCl3

A

Reagents: PCl3
Conditions: Heat

20
Q

Name the reagents and conditions for the preparation of acyl chlorides from carboxylic acids using SOCl2

A

Reagents: SOCl2
Conditions: No Special Conditions

21
Q

Name four reagents that can be used to oxidise methanoic acid and state the observations for each

A

1) Fehling’s: Red Precipitate
2) Tollen’s: Silver mirror
3) Acidified KMnO4: Purple to colourless
4) Acidified K2Cr2O7: Orange to green

22
Q

Name the reagent and conditions that can be used to oxidise ethandioic acid

A

Reagent: Acidified KMnO4
Condition: Warm

*NOTE: Fehling’s and Tollen’s doesn’t work with ethandioic acid

23
Q

Name the reagents and conditions for the formation of secondary amines from primary amines

A

Reagents: Halogenoalkanes
Conditions: In ethanol + heat + pressure

24
Q

Name the reagents and the conditions for the production of amines from amides

A

Reagents: LiAlH4
Conditions: Dry ether

25
Name the reagent and conditions for the formation of amines from nitriles
Reagents: LiAlH4 Conditions: Dry ether or Reagents: H2 Conditions: Ni catalyst
26
Name the reagents and conditions for the formation of phenylamine from nitrobenzene
Reagents: Conc.HCl (followed by NaOH) Conditions: Sn catalyst + Heat under reflux
27
Name the reagents and conditions for the bromination of phenylamine
Reagents: Br2 Conditions: Room Temperature
28
Name the reagents and conditions required for the conversion of alcohols to alkenes
Reagents: Conc. H2SO4 Conditions: Heat
29
Name the products formed from the acidic hydrolysis of amides
1) Carboxylic acid 2) Ammonia (RNH2)
30
Name the products formed from the alkaline hydrolysis of amides
1) Carboxylate salt (COO-Na+) 2) Ammonia
31
Name the reagents and conditions required for the production of nitriles
Reagents: Halogenoalkanes, KCN Conditions Heat
32
Name the reagents and conditions required for the production of hydroxynitriles
Reagents: Aldehydes/Ketones, HCN Conditions: KCN catalyst, heat
33
Name the reagents and conditions for the conversion of nitriles to carboxylic acids
Reagents: dilute acid/alkali + acidification Conditions: Heat